SCHEMBL700798

SCHEMBL700798

COc1cccc(C=Cc2ccccc2)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RELA Q04206 1/20 0.81
NFE2L2 Q16236 4/20 0.73
CYP19A1 P11511 1/20 0.73
CYP1A1 P04798 3/20 0.69
CYP1A2 P05177 3/20 0.69
CYP1B1 Q16678 3/20 0.69
NQO2 P16083 1/20 0.68
TRPA1 O75762 1/20 0.67
TUBB4A P04350 1/20 0.66
TUBB P07437 1/20 0.66
TUBA3C P0DPH7 1/20 0.66
TUBA1B P68363 1/20 0.66
TUBA4A P68366 1/20 0.66
TUBB4B P68371 1/20 0.66
TUBB3 Q13509 1/20 0.66
TUBB2A Q13885 1/20 0.66
TUBB8 Q3ZCM7 1/20 0.66
TUBA3E Q6PEY2 1/20 0.66
TUBA1A Q71U36 1/20 0.66
TUBA1C Q9BQE3 1/20 0.66

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL700797 1.00 RELA (0.81) RELANFE2L2CYP19A1CYP1A1CYP1A2
SCHEMBL14401251 1.00 RELA (0.81) RELANFE2L2CYP19A1CYP1A1CYP1A2
SCHEMBL23158820 0.94 RELA (0.84) RELANFE2L2CYP19A1CYP1A1CYP1A2
SCHEMBL700055 0.94 RELA (0.84) RELANFE2L2CYP19A1CYP1A1CYP1A2
SCHEMBL31317665 0.94 RELA (0.84) RELANFE2L2CYP19A1CYP1A1CYP1A2
SCHEMBL700056 0.94 RELA (0.84) RELANFE2L2CYP19A1CYP1A1CYP1A2
SCHEMBL7592868 0.92 RELA (0.70) RELANFE2L2CYP19A1CYP1A1CYP1A2
SCHEMBL7592867 0.92 RELA (0.70) RELANFE2L2CYP19A1CYP1A1CYP1A2
SCHEMBL699631 0.90 RELA (1.00) RELANFE2L2CYP19A1CYP1A1CYP1A2
SCHEMBL699632 0.90 RELA (1.00) RELANFE2L2CYP19A1CYP1A1CYP1A2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 59 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105669391-A Preparation method of 1-benzyloxy-2-[2-(3-methoxyphenyl)vinyl]benzene 苏州诚和医药化学有限公司 2016-06-15 CN claimed
CN-116637102-B Application of flavane compound in preparation of antitumor drugs 北京中医药大学 2024-04-09 CN disclosed
WO-2021074275-A1 EFFECTIVE PHOTOMODULATION OF LANTHANIDE (III) ION LUMINESCENCE IN THE VISIBLE OR NEAR-INFRARED RANGE UNIVERSITE DE RENNES 1 (FR) 2021-04-22 WO disclosed
US-9925153-B2 Therapeutic agents for skin diseases and conditions STC.UNM (US) 2018-03-27 US disclosed
US-9868873-B2 Photochromic security enabled ink for digital offset printing applications XEROX CORPORATION (US) 2018-01-16 US disclosed
CN-105669391-B A kind of 1 benzyloxy 2 [2(3 methoxyphenyls)Vinyl] benzene preparation method 苏州诚和医药化学有限公司 2018-01-09 CN disclosed
CN-105669391-B A kind of 1 benzyloxy 2 [2(3 methoxyphenyls)Vinyl] benzene preparation method 苏州诚和医药化学有限公司 2018-01-09 CN disclosed
CN-105541569-B A kind of 1 benzyloxy 2 [2(3 methoxyphenyls)Vinyl] benzene synthetic method 苏州诚和医药化学有限公司 2017-11-07 CN disclosed
CN-105218405-B The synthesis technique of (R, S) 2 [[base of 5 (9 fluorenylmethyloxycarbonyl amino) dibenzo [A, D] cycloheptane 2] oxygen] acetic acid 上海泰坦科技股份有限公司 2017-07-28 CN disclosed
US-20160287531-A1 THERAPEUTIC AGENTS FOR SKIN DISEASES AND CONDITIONS STC.UNM 2016-10-06 US disclosed
EP-1591830-A2 Reimageable medium Xerox Corporation (US) 2005-11-02 EP disclosed
EP-1591831-A2 Reimageable medium with light absorbing material Xerox Corporation (US) 2005-11-02 EP disclosed
EP-1591829-A1 Method for forming temporary image Xerox Corporation (US) 2005-11-02 EP disclosed
US-6392111-B1 REACTING AROMATIC COMPOUND WITH OLEFIN STUDIENGESELLSCHAFT KOHLE MBH (DE) 2002-05-21 US disclosed
US-5759729-A A DRY TONER COMPRISING A RESIN, PHOTOCHROMATIC SPIROPYRAN, -OXAZINE OR -THIOPYRAN DYE AND A CHARGE CONTROL AGENT;ELECTROGRAPHY; XEROGRAPHY XEROX CORPORATION (US) 1998-06-02 US disclosed
US-5710420-A Method for embedding and recovering machine-readable information XEROX CORPORATION (US) 1998-01-20 US disclosed
US-5633109-A Ink compositions with liposomes containing photochromic compounds XEROX CORPORATION (US) 1997-05-27 US disclosed
US-5593486-A Photochromic hot melt ink compositions XEROX CORPORATION (US) 1997-01-14 US disclosed
US-5551973-A LIQUID CRYSTAL GEL PHASE, MICROEMULSION PHASE XEROX CORPORATION (US) 1996-09-03 US disclosed
US-5314693-A Hydroxystilbene compounds KIORITZ CORPORATION (JP) 1994-05-24 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20160287531-A1 THERAPEUTIC AGENTS FOR SKIN DISEASES AND CONDITIONS CUTA, TSLP, ELANE RELA 29/4885NFE2L2 696/4885CYP19A1 564/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.